Surface passivation by multifunctional carbon dots toward highly efficient and stable inverted perovskite solar cells

被引:11
|
作者
Cao, Qi [1 ]
Zhang, Yixin [1 ]
Pu, Xingyu [1 ]
Zhao, Junsong [1 ]
Wang, Tong [1 ]
Zhang, Kui [2 ]
Chen, Hui [1 ]
He, Xilai [1 ]
Yang, Jiabao [1 ]
Zhang, Cheng [2 ]
Li, Xuanhua [1 ]
机构
[1] Northwestern Polytech Univ, Ctr Nano Energy Mat, Sch Mat Sci & Engn, State Key Lab Solidificat Proc, Xian 710072, Shaanxi, Peoples R China
[2] Anhui Univ Technol, Sch Chem & Chem Engn, Maanshan 243032, Anhui, Peoples R China
基金
中国国家自然科学基金;
关键词
Interfacial engineering; Carbon dots; Non-radiative recombination; INDUCED DEGRADATION;
D O I
10.1016/j.jechem.2023.07.002
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Interfacial imperfections between the perovskite layer and the electron transport layer (ETL) in perovskite solar cells (PSCs) can lead to performance loss and negatively influence long-term operational stability. Here, we introduce an interface engineering method to modify the interface between perovskite and ETL by using multifunctional carbon dots (CDs). C = O in the CDs can chelate with the uncoordinated Pb2+ in the perovskite material, inhibit interfacial recombination, and enhance the performance and stability of device. In addition, -OH in CDs forms hydrogen bonds with I- and organic cation in perovskite, inhibiting light-induced I2 release and organic cation volatilization, causing irreversible degradation of perovskite films, thereby enhancing the long-term operational stability of PSCs. Consequently, we achieve the champion inverted device with an efficiency of 24.02%. The CDs-treated PSCs exhibit high operational stability, and the maximum power point tracking only attenuates by 12.5% after 1000 h. Interfacial modification engineering supported by multifunctional quantum dots can accelerate the road to stable PSCs. (c) 2023 Science Press and Dalian Institute of Chemical Physics, Chinese Academy of Sciences. Published by ELSEVIER B.V. and Science Press. All rights reserved.
引用
收藏
页码:9 / 15
页数:7
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